Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:18194843-18194965 | Rare:63 | ||||
chr19:18279635-18279722 | Rare:34 | ||||
chr19:19776378-19776591 | Common:2; Rare:58 | ||||
chr19:20423670-20423727 | Rare:15 | ||||
chr19:20432269-20432626 | Common:8; Rare:91 | ||||
chr19:21440625-21440902 | Rare:38 | ||||
chr19:21569237-21569392 | Common:6; Rare:43 | ||||
chr19:27793350-27793471 | Common:2; Rare:32 | ||||
chr19:27793667-27794035 | Rare:95 | ||||
chr19:33176861-33177053 | Common:8; Rare:98 | ||||
chr19:36331631-36331869 | Common:2; Rare:67 | ||||
chr19:36797259-36797554 | Common:1; Rare:63 | ||||
chr19:38714330-38714552 | Common:2; Rare:54; Clinvar (benign):1 | ||||
chr19:39409648-39409856 | Common:1; Rare:52 | ||||
chr19:39410525-39410759 | Common:1; Rare:50 |